Detalhe da pesquisa
1.
Novel PIK3CD mutations affecting N-terminal residues of p110δ cause activated PI3Kδ syndrome (APDS) in humans.
J Allergy Clin Immunol;
140(4): 1152-1156.e10, 2017 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28414062
2.
Human PI3Kγ deficiency and its microbiota-dependent mouse model reveal immunodeficiency and tissue immunopathology.
Nat Commun;
10(1): 4364, 2019 09 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31554793